Canonical Allele Identifier: CA406013622

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41422948-C-T
• MyVariant Identifiers: chr19:g.41928853C>T (hg19) ; chr19:g.41422948C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422948C>T , CM000681.2:g.41422948C>T	GRCh38
NC_000019.9:g.41928853C>T , CM000681.1:g.41928853C>T	GRCh37
NC_000019.8:g.46620693C>T	NCBI36
NG_013004.1:g.30160C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.996-50C>T MANE Select	ENSP00000269980.2:n.996-50C>T
ENST00000269980.6:c.996-50C>T	ENSP00000269980.2:n.996-50C>T
ENST00000457836.6:c.955C>T	ENSP00000416000.2:p.Pro319Ser
ENST00000540732.3:c.1098-50C>T	ENSP00000443246.1:n.1098-50C>T
ENST00000542943.5:c.909-50C>T	ENSP00000440345.1:n.909-50C>T
ENST00000595085.5:c.922+251C>T	ENSP00000471150.2:n.922+251C>T
NM_000709.3:c.996-50C>T	NP_000700.1:n.996-50C>T
NM_001164783.1:c.993-50C>T	NP_001158255.1:n.993-50C>T
NM_000709.4:c.996-50C>T MANE Select	NP_000700.1:n.996-50C>T
NM_001164783.2:c.993-50C>T	NP_001158255.1:n.993-50C>T